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RAVISRO Study - Postoperative Outcomes of Radical Visceral resections in Oncosurgery

Postoperative outcomes of oncology patients undergoing radical visceral resections - a multi-centric observational study (RaVisRO study). - RAVISRO

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/08/072057
Enrollment
500
Registered
2024-08-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C260- Malignant neoplasm of intestinal tract, part unspecified

Interventions

Control Intervention1: NIL: NIL

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: All patients aged 18 years and above who are undergoing elective onco-surgical procedures that involve radical visceral resections and are shifted postoperatively to the surgical ICU. 1) Cytoreductive surgery (CRS) plus Hyperthermic Intraperitoneal Chemotherapy (HIPEC) 2) Transthoracic esophagectomy (TTE) plus 3-field lymph node dissection 3) Hepatectomy 4) Parenchyma-sparing liver metastatectomy 5) Radical cholecystectomy 6) Extrahepatic biliary tree excision 7) Whipple’s procedure with or without vascular reconstruction 8) Retroperitoneal sarcoma excision 9) Pelvic exenteration surgery

Exclusion criteria

Exclusion criteria: Redo surgeries that involve radical visceral resections within 30 days of primary surgery will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
Incidence of Clavien-Dindo postoperative complications and the Comprehensive Complication Index (CCI)Timepoint: at discharge and at 30 days

Secondary

MeasureTime frame
Morbidity predictorsTimepoint: 90 days

Countries

India

Contacts

Public ContactDr Deepa Chandramohan

MVR Cancer Centre and Research Institute

drdeepac@mvrccri.co7012035765

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026